SMB00807

Glycolithocholate sulfate

≥95% (HPLC)

• 別名: Glycolithocholic acid 3-sulfate, Sulfoglycolithocholic acid, Sulfolithocholylglycine
• 実験式（ヒル表記法）: C₂₆H₄₃NO₇S
• CAS番号: 15324-64-8
• 分子量: 513.69
• UNSPSCコード: 41141802
• NACRES: NA.28

特性

• アッセイ: ≥95% (HPLC)
• 輸送温度: wet ice
• 保管温度: −20°C
• SMILES記法: [S](=O)(=O)([O-])O[C@H]1C[C@@H]2[C@@]([C@@H]3[C@H]([C@H]4[C@@]([C@H](CC4)[C@@H](CCC(=O)NCC(=O)O)C)(CC3)C)CC2)(CC1)C
• InChI: 1S/C26H43NO7S/c1-16(4-9-23(28)27-15-24(29)30)20-7-8-21-19-6-5-17-14-18(34-35(31,32)33)10-12-25(17,2)22(19)11-13-26(20,21)3/h16-22H,4-15H2,1-3H3,(H,27,28)(H,29,30)(H,31,32,33)/p-1/t16-,17-,18-,19+,20-,21+,22+,25+,26-/m1/s1
• InChI Key: FHXBAFXQVZOILS-OETIFKLTSA-M

詳細

詳細

Sulfoglycolithocholic acid, also known as sulfolithocholylglycine, belongs to the class of compounds referred as glycinated bile acids and derivatives. This compound serves as a valuable asset in both biochemical and metabolomics research due to its significant role in the field of bile acid conjugates and secondary bile acid production. Sulfolithocholylglycine is the 3-O-sulfo derivative of glycolithocholic acid and is synthesized through microbial flora enzymes in the colonic environment. In hepatocytes, bile acids, both primary and secondary, undergo amino acid conjugation at the C-24 carboxylic acid on the side chain, resulting in the predominance of glycine-conjugated forms of bile acids in the bile duct[1]. This compound′s unique properties make it an intriguing subject for research, with potential applications in metabolomics and biochemistry.

アプリケーション

Sulfoglycolithocholic acid can be used in biochemical research and metabolomics research. It can be used to study the metabolism of bile acids, the gut microbiome, and the effects of bile acids on various tissues and organs.

特徴および利点

• Can be used in Metabolomics and Biochemical research
• High-quality compound suitable for multiple research applications

その他情報

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安全性情報

• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable